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>Home >FACULTY> Hsiao-Chun Huang, Assistant Professor
Hsiao-Chun Huang, Assistant Professor
 
Assistant Professor

Born in 1980

Ph. D. U.S.A Harvard University, U.S.A..
Specialty: cell division, systems and synthetic biology

E-mail : hsiaochun@ntu.edu.tw

Laboratory: Life Science Building R738

TEL 886-2- 33662481 FAX 886-2-33662478

Recent Research Topics
  • Spindle scaling and orientation in normal and cancer cells

  • Synthetic polarity and asymmetric cell division in E. coli

  • Cellular reprogramming by small molecules

Laboratory: Laboratory of Systems and Synthetic Biology

Cell division and differentiation are among the most fundamental and fascinating processes in life. Perturbation of these processes can lead to cancerous proliferation and heterogeneity (or, beneficial survival for single-cell organisms). The lab uses mammalian and bacterial cells as our model systems; microscopy, small molecules, synthetic biology and computation as our primary approaches. We attempt to understand how governing molecules and quantitative scaling parameters are involved in symmetric/asymmetric divisions and differentiation, and how reconstruction may pave novel ways for therapies and applications.

 

Selected Research Publications

Wang WL, Huang HC, Kao SH, Hsu YC, Wang YT, Li KC, Chen YJ, Yu SL, Wang SP, Hsiao TH, Yang PC, Hong TM. Slug is temporally regulated by cyclin E in cell cycle and controls genomic stability. (Oncogene 2014 Mar 24. doi:10.1038/ onc.2014.58. [Epub ahead of print])

 

Pan CJ and Huang HC*. (2013). Noise in Genetic Circuits: Hindrance or Chance? IEEE/ACM International Conference on Computer-Aided Design (ICCAD, special session paper). (*Corresponding author)

 

Kwiatkowski N, Deng X, Wang J, Tan L, Villa F, Santaguida S, Huang HC, Mitchison T, Musacchio A, Gray N. (2012). Selective Aurora Kinase Inhibitors Identified Using a Taxol-Induced Checkpoint Sensitivity Screen. ACS Chem Biol. 7 , 185-96.

 

Shi J, Zhou I, Huang HC and Mitchison TJ. (2011). Navitoclax (ABT-263) accelerates apoptosis during drug-induced mitotic arrest by antagonizing Bcl-xL. Cancer Research 71 , 4518-26.

 

Huang HC, Mitchison TJ and Shi J. (2010). Stochastic competition between mechanistic independent slippage and death pathways determines cell fate during mitotic arrest. PLoS ONE 5 , e15724.

 

Huang HC*, Shi J, Orth JD and Mitchison TJ. (2010). Cell death when the SAC is out of commission. Cell Cycle 9 , 2049-50. (*Corresponding author)

 

Huang HC*, Shi J, Orth JD and Mitchison TJ. (2009). Evidence that mitotic exit is a better cancer therapeutic target than spindle assembly. Cancer Cell 16 , 347-58. (*Corresponding author)

 

 


Courses Information

MCB7026 Systems and Synthetic Approaches to Biology
MCB7025 Seminar in Systems and Synthetic Biology
MCB7002 Research Training 
MCB7002 Molecular Cell Biology
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